DailyMed label
buprenorphine
DailyMed label · PAYLESS COMPOUNDERS, LLC · version 10
Key facts
| Product | buprenorphine |
|---|---|
| Labeler | PAYLESS COMPOUNDERS, LLC |
| Document type | ANIMAL COMPOUNDED DRUG LABEL |
| Active ingredients | BUPRENORPHINE HYDROCHLORIDE |
| Active ingredient UNIIs | 56W8MW3EN1 |
| Route | INTRAMUSCULAR, SUBCUTANEOUS, ORAL, TRANSMUCOSAL |
| DEA schedule | CIII |
| NDC package codes | 70022-001-10, 70022-004-10, 70022-010-03, 70022-010-10 |
| Effective date | Dec 11, 2024 |
| Set ID | a1c1f498-e101-467f-b81c-1451c44e7a01 |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: